Stereocontrolled Total Synthesis of (5S,6R)-, (5S,6S)-, (5R,6R)-, and (5R,6S)(7E,9E,11Z,14Z)-5,6-Dihydroxy-7,9,11,14-icosatetraenoic Acid (5,6-DiHETE) Methyl Esters-Reference-Cited by-同舟云学术

Stereocontrolled Total Synthesis of (5S,6R)-, (5S,6S)-, (5R,6R)-, and (5R,6S)(7E,9E,11Z,14Z)-5,6-Dihydroxy-7,9,11,14-icosatetraenoic Acid (5,6-DiHETE) Methyl Esters

Published:1989-05 Issue:5 Volume:28 Page:587-588
ISSN:0570-0833
Container-title:Angewandte Chemie International Edition in English
language:en
Short-container-title:Angew. Chem. Int. Ed. Engl.

Author:

Nicolaou K. C.,Ramphal J. Y.,Palazon J. M.,Spanevello R. A.

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference13 articles.

1. Leukotriene A4. Enzymatic conversion into 5,6-dihydroxy-7,9,11,14-eicosatetraenoic acid by mouse liver cytosolic epoxide hydrolase.

2. Metabolism of arachidonic acid in polymorphonuclear leukocytes. Structural analysis of novel hydroxylated compounds.

3. Enzymatic formation of 5,6-dihydroxy-7,9,11,14-eicosatetraenoic acid: kinetics of the reaction and stereochemistry of the product

4. Enantiospecific and stereospecific synthesis of lipoxin A. Stereochemical assignment of the natural lipoxin A and its possible biosynthesis

5. Lipoxins: novel series of biologically active compounds formed from arachidonic acid in human leukocytes.

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